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Results 1 to 25 of 559

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Silent point mutation in DsRed resulting in enhanced relative fluorescence intensityKLASEN, Maik; WABL, Matthias.BioTechniques. 2004, Vol 36, Num 2, pp 236-238, issn 0736-6205, 2 p.Article

High level of gene silencing in the tetraploid goldfishWOODS, T. D; BUTH, D. G.Biochemical systematics and ecology. 1984, Vol 12, Num 4, pp 415-421, issn 0305-1978Article

Evidence that natural selection acts on silent mutationCONRAD, M; FRIEDLANDER, C; GOODMAN, M et al.Biosystems. 1983, Vol 16, Num 2, pp 101-111, issn 0303-2647Article

Glyoxalase I null allele in a new family: identification by abnormal segregation pattern and quantitative assaySPARKES, R. S; SPARKES, M. C; CRIST, M et al.Human genetics. 1983, Vol 64, Num 2, pp 146-147, issn 0340-6717Article

Inheritance of the human salivary proline-rich proteins: a reinterpretation in terms of six loci forming two subfamiliesMAEDA, N.Biochemical genetics. 1985, Vol 23, Num 5-6, pp 455-464, issn 0006-2928Article

On the time for gene silencing at duplicate lociWATTERSON, G. A.Genetics. 1983, Vol 105, Num 3, pp 745-766, issn 0016-6731Article

Detection of electrophoretically silent mutations by immobilized pH gradientsCOSSU, G; MANCA, M; STRAHLER, J. R et al.Journal of chromatography. 1986, Vol 361, pp 223-229, issn 0021-9673Article

Occurrence of a rare allele at the Est-6 locus in natural populations of Drosophila melanogasterCAMBISSA, V; NIGRO, L; DANIELI, G. A et al.Bollettino di Zoologia. 1982, Vol 49, Num 3-4, pp 229-233, issn 0373-4137Article

Interaction of silent and replacement changes in eukaryotic coding sequencesLIPMAN, D. J; WILBUR, W. J.Journal of molecular evolution. 1984, Vol 21, Num 2, pp 161-167, issn 0022-2844Article

Three japanese families with members carrying C7 silent allele (C7*QO). Possibility for an association between C7*QO and C6*B1NISHIMUKAI, H; KITAMURA, H; TAKEUCHI, Y et al.Human heredity. 1988, Vol 38, Num 4, pp 246-250, issn 0001-5652Article

Induction of alcohol dehydrogenase null mutants in the Mediterranean fruit fly Ceratitis capitataRIVA, M. E; ROBINSON, A. S.Biochemical genetics. 1986, Vol 24, Num 9-10, pp 765-774, issn 0006-2928Article

PGMI null allele detected in a Caucasian mother-son pairWARD, L. J; ELSTON, R. C; KEATS, B. J. B et al.Human heredity. 1985, Vol 35, Num 3, pp 178-181, issn 0001-5652Article

Genetic hitchhiking and the evolution of reduced genetic activity of the Y sex chromosomeRICE, W. R.Genetics. 1987, Vol 116, Num 1, pp 161-167, issn 0016-6731Article

The protein burden of lac operon productsKOCH, A. L.Journal of molecular evolution. 1983, Vol 19, Num 6, pp 455-462, issn 0022-2844Article

STUDIES OF ESTERASE 6 IN DROSOPHILA MELANOGASTER. VII: REMATING TIMES OF FEMALES INSEMINATED BY MALES HAVING ACTIVE OR NULL ALLELESGILBERT DG; RICHMOND RC; SHEEHAN KB et al.1981; BEHAV. GENET.; ISSN 0001-8244; USA; DA. 1981; VOL. 11; NO 3; PP. 195-208; BIBL. 2 P.Article

ADENOSINE DEAMINASE POLYMORPHISM. ASSOCIATIONS AT CLINICAL LEVEL SUGGEST A ROLE IN CELL FUNCTIONS AND IMMUNE REACTIONSBOTTINI E; CARAPELLA E; CATALDI L et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 5; PP. 331-334; BIBL. 16 REF.Article

Heterogeneity of the silent gene for plasma cholinesterase : immunological studiesWHITTAKER, M; JONES, J; BRAVEN, J et al.Human heredity. 1990, Vol 40, Num 3, pp 153-158, issn 0001-5652Article

Mutations leading to expression of the cryptic HMRa locus in the yeast Saccharomyces cerevisiaeKASSIR, Y; SIMCHEN, G.Genetics. 1985, Vol 109, Num 3, pp 481-492, issn 0016-6731Article

Génétique et évolution du système Lpm. II. Apparition instantanée du polymorphisme des allotypes Lpm chez le vison domestique comme résultat possible de l'activation phylogénétique de gènes silencieuxBELYAEV, D. K; BARANOV, O. K; ERMOLAEV, V. I et al.Genetika. 1984, Vol 20, Num 1, pp 128-139, issn 0016-6758Article

Object-oriented bayesian networks for complex forensic DNA profiling problemsDAWID, A. P; MORTERA, J; VICARD, P et al.Forensic science international. 2007, Vol 169, Num 2-3, pp 195-205, issn 0379-0738, 11 p.Article

HUMAN NEUTRAL ALPHA -GLUCOSIDASE C: GENETIC POLYMORPHISM INCLUDING A "NULL" ALLELEMARTINIUK F; HIRSCHHORN R.1980; AMER. J. HUM. GENET.; USA; DA. 1980; VOL. 32; NO 4; PP. 497-507; BIBL. 31 REF.Article

EVIDENCE FOR A NULL ALLELE AT THE ESTERASE D (EC 3.1.1.1) LOCUSSPARKES RS; TARGUM S; GERSHON E et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 319-323; BIBL. 4 REF.Article

A NEW CASE OF A SILENT ALLELE IN THE PGM1 SYSTEMHERZOG P; LIBICH M.1982; HUMAN HEREDITY; ISSN 0001-5652; CHE; DA. 1982; VOL. 32; NO 4; PP. 293-295; BIBL. 5 REF.Article

NULL MUTANTS OF THE A AND A MATING TYPE ALLELES OF NEUROSPORA CRASSAGRIFFITHS AJF.1982; CANADIAN JOURNAL OF GENETICS AND CYTOLOGY; ISSN 0008-4093; CAN; DA. 1982; VOL. 24; NO 2; PP. 167-176; ABS. FRE; BIBL. 20 REF.Article

A NULL ALLELE AT THE MOD-1 LOCUS OF THE MOUSEJOHNSON FM; CHASALOW F; LEWIS SE et al.1981; J. HERED.; ISSN 0022-1503; USA; DA. 1981; VOL. 72; NO 2; PP. 134-136; BIBL. 20 REF.Article

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